Canonical Allele Identifier: CA16042784
Gene: TBX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 372527
ClinVar RCV Id: RCV000413700
dbSNP Id: rs1057517833

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114385561G>A , CM000674.2:g.114385561G>A GRCh38
NC_000012.11:g.114823366G>A , CM000674.1:g.114823366G>A GRCh37
NC_000012.10:g.113307749G>A NCBI36
NG_007373.1:g.27882C>T , LRG_670:g.27882C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405440.7:c.670C>T MANE Select ENSP00000384152.3:p.Gln224Ter
ENST00000310346.8:c.670C>T ENSP00000309913.4:p.Gln224Ter
ENST00000349716.9:c.520C>T ENSP00000337723.5:p.Gln174Ter
ENST00000405440.6:c.670C>T ENSP00000384152.2:p.Gln224Ter
ENST00000526441.1:c.670C>T ENSP00000433292.1:p.Gln224Ter
NM_000192.3:c.670C>T , LRG_670t1:c.670C>T NP_000183.2:p.Gln224Ter
NM_080717.2:c.520C>T NP_542448.1:p.Gln174Ter
NM_181486.2:c.670C>T NP_852259.1:p.Gln224Ter
XM_017019912.1:c.718C>T XP_016875401.1:p.Gln240Ter
NM_080717.3:c.520C>T NP_542448.1:p.Gln174Ter
NM_181486.4:c.670C>T MANE Select NP_852259.1:p.Gln224Ter
NM_080717.4:c.520C>T NP_542448.1:p.Gln174Ter